- Open Access
Profiling of the anti-malarial drug candidate SC83288 against artemisinins in Plasmodium falciparum
© The Author(s) 2018
- Received: 28 November 2017
- Accepted: 15 March 2018
- Published: 20 March 2018
The increased resistance of the human malaria parasite Plasmodium falciparum to currently employed drugs creates an urgent call for novel anti-malarial drugs. Particularly, efforts should be devoted to developing fast-acting anti-malarial compounds in case clinical resistance increases to the first-line artemisinin-based combination therapy. SC83288, an amicarbalide derivative, is a clinical development candidate for the treatment of severe malaria. SC83288 is fast-acting and able to clear P. falciparum parasites at low nanomolar concentrations in vitro, as well as in a humanized SCID mouse model system in vivo. In this study, the antiplasmodial activity of SC83288 against artemisinins was profiled in order to assess its potential to replace, or be combined with, artemisinin derivatives.
Based on growth inhibition and ring survival assays, no cross-resistance was observed between artemisinins and SC83288, using parasite lines that were resistant to either one of these drugs. In addition, no synergistic or antagonistic interaction was observed between the two drugs. This study further confirmed that SC83288 is a fast acting drug in several independent assays. Combinations of SC83288 and artesunate maintained the rapid parasite killing activities of both components.
The results obtained in this study are consistent with artemisinins and SC83288 having distinct modes of action and different mechanisms of resistance. This study further supports efforts to continue the clinical development of SC83288 against severe malaria as an alternative to artemisinins in areas critically affected by artemisinin-resistance. Considering its fast antiplasmodial activity, SC83288 could be combined with a slow-acting anti-malarial drug.
- Plasmodium falciparum
- Anti-malarial drug
- Severe malaria
- Drug development
- Artemisinin-based combination therapy
SC83288, an amicarbalide derivative, is active against P. falciparum blood stages at low nanomolar concentrations in vitro, with IC50 values of 3 nM. SC83288 is able to clear a P. falciparum infection in a humanized NOD/SCID mouse model system within 48 h following intraperitoneal injections of 2.5 mg kg−1 once per day over a period of 3 days . Furthermore, SC83288 is fast acting and it has favourable pharmacological and toxicological features . In vitro resistance to SC83288 develops slowly and might involve mutational changes in the Ca2+ transporting PfATP6, the P. falciparum SERCA orthologue. However, PfATP6 does not seem to be the molecular target of SC83288 but rather a component of resistance .
PfATP6 is a validated drug target  and was once considered the prime molecular target of artemisinins [22–25] and a contributor to artemisinin resistance [26–29]. However, recent studies failed to detect a specific interaction between PfATP6 and artemisinins [30–35], and instead favour a pleiotropic mode of action in that many proteins are covalently modified by the alkylating property of artemisinins . Moreover, resistance to artemisinins has recently been associated with polymorphisms in the kelch propeller domain protein 13 (PfK13) [37–46], a member of the kelch protein superfamily, bearing multiple protein–protein interaction sites and involved, among others, in ubiquitin-regulated protein degradation and oxidative stress responses .
Considering the gold standard status of artemisinin and its derivatives in the anti-malarial drug development field and taking into account that PfATP6 has repeatedly been considered a drug target of, or a contributor to drug resistance, including to SC83288, raises the possibility that SC83288 and artemisinins exert their antiplasmodial activity, or induce resistance, in P. falciparum in a similar or synergistic manner. The data presented herein suggest that these concerns are unfounded. No cross-resistance was observed between dihydroartemisinin and SC83288 in vitro. Moreover, both drugs showed neither a synergistic nor antagonistic interaction. Consistent with previous results, SC83288 was found to be a fast acting compound, although SC83288 is not as rapid regarding its in vitro speed of action as are artemisinins . Furthermore, combining SC83288 with artesunate did not affect the in vitro speed of action of either drug, allowing for the possibility of a combination therapy.
The chemicals used in this study were obtained from the Roth, Merck, Sigma, Serva, Thermo and Applichem. SC83288 was provided by the 4SC AG, München, Germany.
Plasmodium falciparum parasites were maintained in continuous in vitro culture essentially as previously described . Briefly, cultures were maintained at a haematocrit of 5.0% and at a parasitaemia of not higher than 5% (if not stated otherwise) in RPMI 1640 supplemented with 2 mM l-glutamine, 25 mM HEPES, 100 µM hypoxanthine, 20 µg ml−1 gentamycin, 5% human heat-inactivated AB-positive serum and 5% Albumax. Cultures were incubated at 37 °C under controlled atmospheric conditions of 5% O2, 3% CO2, 92% N2 and 96% humidity. Synchronization of cultures at the ring stage was performed using a 5% sorbitol solution as previously described .
Plasmodium falciparum growth inhibition assay
Growth inhibition assays were performed according to a standardized protocol, based on the detection of parasite DNA by fluorescent SYBRGreen staining [50, 51]. Briefly, synchronized cultures of P. falciparum ring-stage parasites were incubated in the presence of increasing drug concentrations, at the following final condition: 100 µl per well, 0.5% parasitaemia, 2% haematocrit, 72 h incubation at 37 °C. After incubation, the plates were frozen at − 80 °C overnight. On the day of the measurement, plates were thawed for 1 h at room temperature. The plates were filled with 100 µl per well of a 1× SYBRGreen (ThermoFisher Scientific Inc.) solution in lysis buffer (H20, 20 mM Tris base pH 7.4, 5 mM EDTA, 0.008% (w/v) Saponin, 0.08% (w/v) Triton X-100), briefly shaken and incubated at room temperature for 1 h. Plates were protected from direct light. Fluorescence was measured in a fluorescence plate reader (FluoStar Optima, BMG Labtech GmbH) (ext/em: 485/520 nm, gain 1380, 10 flashes/well, top optic). The IC50 values were calculated using a four parameter sigmoidal function (SigmaPlot 13, Systat Software Inc.). 6–13 independent biological replicates were performed, each with technical duplicates.
Ring survival assay
Drug interaction study
The interaction profile was assessed using the P. falciparum strain Dd2 and the fixed-ratio isobologram method . This approach is based on determining the IC50 values of two individual drugs alone and in combination at different concentration ratios. In principle, the shift of a drug’s IC50 value, assessed in combination compared to the one determined for this drug alone, is indicative of the nature of the interaction between the two drugs . Briefly, a synchronous culture of ring-stage P. falciparum blood-stage parasites was incubated for 72 h in the presence of increasing drug concentrations in a 96-well black microtiter plate. The final conditions of the tests were 100 µl per well, 0.5% parasitaemia, 2% final haematocrit and 72 h incubation time at 37 °C. On the day of the assay, a synchronized ring-stage culture, was established at 0.5% parasitaemia and 4% haematocrit. A solution of uninfected erythrocytes at 4% haematocrit was used as a negative control. Drugs were applied alone (A or B) and in combination at fixed concentration ratios (A:B) and analysed in threefold serial dilutions. Drug mixtures were prepared from 2x working solutions of each drug in the following fixed concentration ratios (v/v): ratio A:B = 4:1, 3:2, 2.5:2.5, 2:3, 1:4, directly in the 96-well plate. IC50 values of drugs A and B alone were determined on the same plate to ensure accurate calculation of drug interactions. After 72 h of incubation, plates were wrapped in aluminum foil and frozen at − 80 °C overnight. Parasite growth was assessed using SYBRGreen as described above. Graphical analysis was performed on isobolograms, obtained by plotting pairs of fractional IC50 (FIC50) values of drug A and drug B for each combination. The in vitro interactions were evaluated based on graphical and arithmetical analysis. It is commonly accepted that a mean sum of fractional 50% inhibitory concentrations (mean ∑FIC50) lower than 0.5 corresponds to a synergistic interaction, and higher than 1.5 to an antagonistic interaction . A mean ∑FIC50 between these two cut-off values represents an indifferent interaction between the two investigated drugs. 7 independent biological replicates were performed, each with technical duplicates.
In vitro speed of action
SC83288 shows no cross-resistance with artemisinins
The matter of cross-resistance between SC83288 and artemisinins was initially addressed, using two distinct approaches. On the one hand, standard growth inhibition assays over 72 h of drug exposure were performed, and on the other hand, the susceptibility of early ring stages in a ring survival assay (RSA) was evaluated. The RSA takes into account the antiplasmodial activity of artemisinin and its derivatives against the early blood stages [36, 52]. Four different strains of P. falciparum were used in these assays: the artemisinin and SC83288 sensitive P. falciparum strains NF54 and Dd2, the genetically engineered artemisinin-resistant NF54 mutant line bearing a mutation in the kelch 13 gene (PfK13 C580Y), an established marker of artemisinin resistance , and a Dd2 derived SC83288 resistant line . The two drug resistant clones were termed NF54ART and Dd2SC.
Susceptibility of NF54, NF54ART, Dd2, and Dd2SC to SC83288 and artemisinin
5.1 ± 0.7
0.7 ± 0.1
4.9 ± 0.8
0.5 ± 0.1
3.1 ± 0.2
0.7 ± 0.1
1000 ± 200*
0.5 ± 0.5
SC83288 and artemisinin do not interact
Combining SC83288 and artesunate does not affect the in vitro speed of action
Understanding the mode of action and the mechanism of resistance of a therapeutic agent is not mandatory for a compound to be released on the market. However, information regarding these processes may help to predict and control interactions of the compound with the environment and with other drugs deployed in the field. To this purpose, the antiplasmodial action of SC83288 was profiled against artemisinin and artemisinin derivatives in P. falciparum.
The parasite reduction ratio after a single dose, i.e. the speed of action of the molecule, is a quality feature of an anti-malarial drug as recently emphasized by the Medicine for Malaria Venture (MMV) . Particularly, drugs against severe malaria are expected to rapidly clear sequestered parasites from the patient´s microvasculature, which can make the difference between survival and death. Moreover, fast-acting anti-malarial drugs are favoured for their ability to reduce the risks of resistant parasites arising within the patient. To this day, the artemisinin derivatives remain the gold standards of a rapidly clearing anti-malarial, reducing the parasite burden within hours . SC83288 has previously been characterized as a fast-acting anti-malarial compound in vitro  using a recrudescence assay . Under these conditions, the SC83288 speed of action profile was closer to the fast-acting artemisinin than to the slow-acting atovaquone, although the SC83228 showed a slightly longer clearance time and a lower parasite reduction ratio compared to artemisinin . On a direct clearance-time measurement using trophozoites, SC83288, however, revealed a higher activity than artemisinin , consistent with the potent antiplasmodial activity of SC83288 on trophozoites . In this study, the killing speed of SC83288 was verified, using two other methods: a relative speed assay , and a re-invasion assay . The results of these assays were consistent with previous observations, marking SC83288 as a fast-acting anti-malarial compound (Figs. 5 and 6), with an in vitro killing speed profile closer to artesunate than to atovaquone (Fig. 6). Further, combining SC83288 with artesunate did not significantly impair the speed of action (Fig. 6). The speed of action is, however, not the only crucial aspect that needs to be taken into account when developing an anti-malarial compound. As for any xenobiotic molecule, the beneficial versus adverse effects must be carefully weighed, and parameters such as safety, pharmacokinetics and drug–drug interactions need to be considered. In this regard, preliminary results on the safety and toxicology of SC83288 in mice and dogs are promising, although a full assessment would await clinical trials in humans. This study further revealed no obvious in vitro interactions between artemisinin and SC83288 in the P. falciparum strain Dd2 (Fig. 4). Both the graphical and arithmetical analysis of our isobologram method supported this observation, with the isobologram following a linear trend, and a mean sum of fractional 50% inhibitory concentration falling within the range of an indifferent interaction . An isobologram may overlook possible similar modes of action, particularly if the two tested compounds are both either competitive inhibitors or mutually exclusive non-competitive inhibitors . Competition of both compounds for the same binding site, independently of an interference with the binding site of the endogenous substrate, would not be noticed in an isobologram . However, the chemical and structural differences between SC83288 and the artemisinins (Fig. 1) strongly argue against this possibility.
Resistance is another key aspect of the MMV’s drug candidate profile. Indeed, resistance to most marketed anti-malarial drugs, either previously or still currently used to treat a P. falciparum infection, has been identified worldwide to various degrees [62, 63]. Thus, novel drugs need to overcome existing mechanisms of resistance. A previous study has shown that SC83288 is active in vitro against various P. falciparum laboratory strains that are resistant to quinoline, quinoline-like and antifolate anti-malarials . This study extends these findings to include the artemisinin resistant parasite strain NF54ART that carry the kelch 13 mutation associated with reduced artemisinin responsiveness. SC83288 was found to be active against NF54ART. Conversely, resistance to SC83288 did not affect the susceptibility of the parasite to other anti-malarial drugs, including artemisinins, chloroquine, mefloquine and the folate antagonists .
While this study does not provide molecular insights into the precise mode of action of SC83288, or into the possible mechanism of resistance, our study suggests that artemisinins and SC83288 target different molecular pathways, based on the absence of cross-reactivity in several independent assays. The absence of cross-resistance and the ability to break established resistances against several anti-malarial drugs, together with a fast in vitro parasite killing speed, are favourable features of SC83288 and would support further development of this compound, possibly as a treatment against severe malaria. Whether SC83288 can be an alternative to artesunate for the treatment of severe malaria, however, has to await clinical safety and efficacy trials in humans.
MD, CPS, and ML designed this study, MD and ML analysed the data and wrote the manuscript. CPS generated the SC83288 resistant P. falciparum strain. MD performed the experimental work. All authors read and approved the final manuscript.
We thank Marina Müller and Stefan Prior for excellent technical assistance. We are grateful to Prof. Marcel Deponte for advices and guidance. We thank Prof. Alexander Dalpke for allowing us to use his group´s flow cytometer. We are thankful to Dr. Stefanie Fehler for the SC83288 supply and the coordination with the 4SC AG.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets and analysis algorithm used during the current study are available from the corresponding author on reasonable request.
Consent for publication
Ethics approval and consent to participate
The research leading to these results has received funding from the Bundesministerium für Bildung und Forschung under the portfolio of the German Centre for Infectious Research (DZIF) (Project TTU 03.803).
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